Centre for Oral Immunobiology and Regenerative Medicine, Institute of Dentistry, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, Newark Street, London E1 2AT, UK.
Department of Oral Diagnostic Sciences, Division of Oral Pathology and Medicine, Faculty of Dentistry, King Abdul Aziz University, Jeddah 21589, Saudi Arabia.
Int J Mol Sci. 2022 Jun 6;23(11):6349. doi: 10.3390/ijms23116349.
Vimentin, a type III intermediate filament protein, is found in most cells along with microfilaments and microtubules. It has been shown that the head domain folds back to associate with the rod domain and this association is essential for filament assembly. The N-terminally tagged vimentin has been widely used to label the cytoskeleton in live cell imaging. Although there is previous evidence that EGFP tagged vimentin fails to form filaments but is able to integrate into a pre-existing network, no study has systematically investigated or established a molecular basis for this observation. To determine whether a tag would affect de novo filament assembly, we used vimentin fused at the N-terminus with two different sized tags, AcGFP (239 residues, 27 kDa) and 3 × FLAG (22 residues; 2.4 kDa) to assemble into filaments in two vimentin-deficient epithelial cells, MCF-7 and A431. We showed that regardless of tag size, N-terminally tagged vimentin aggregated into globules with a significant proportion co-aligning with β-catenin at cell-cell junctions. However, the tagged vimentin aggregates could form filaments upon adding untagged vimentin at a ratio of 1:1 or when introduced into cells containing pre-existing filaments. The resultant filament network containing a mixture of tagged and untagged vimentin was less stable compared to that formed by only untagged vimentin. The data suggest that placing a tag at the N-terminus may create steric hinderance in case of a large tag (AcGFP) or electrostatic repulsion in case of highly charged tag (3 × FLAG) perhaps inducing a conformational change, which deleteriously affects the association between head and rod domains. Taken together our results shows that a free N-terminus is essential for filament assembly as N-terminally tagged vimentin is not only incapable of forming filaments, but it also destabilises when integrated into a pre-existing network.
波形蛋白是一种 III 型中间丝蛋白,与微丝和微管一起存在于大多数细胞中。已经表明,头部结构域折叠回与杆状结构域结合,这种结合对于丝组装是必不可少的。带有 N 端标签的波形蛋白已广泛用于标记活细胞成像中的细胞骨架。尽管以前有证据表明 EGFP 标记的波形蛋白不能形成纤维,但能够整合到预先存在的网络中,但没有研究系统地调查或建立这种观察结果的分子基础。为了确定标签是否会影响从头组装纤维,我们使用 N 端融合有两种不同大小标签的波形蛋白,AcGFP(239 个残基,27 kDa)和 3×FLAG(22 个残基;2.4 kDa),在两种波形蛋白缺陷的上皮细胞 MCF-7 和 A431 中组装成纤维。我们表明,无论标签大小如何,N 端标记的波形蛋白聚集到球蛋白中,其中很大一部分与β-连环蛋白在细胞-细胞连接处共定位。然而,标记的波形蛋白聚集体可以在添加未标记的波形蛋白的比例为 1:1 时或在引入含有预先存在的纤维的细胞中形成纤维。与仅由未标记的波形蛋白形成的纤维网络相比,包含标记和未标记的波形蛋白混合物的纤维网络的稳定性较低。该数据表明,在大标签(AcGFP)的情况下,在 N 端放置标签可能会产生空间位阻,或者在带高电荷的标签(3×FLAG)的情况下可能会产生静电排斥,从而可能诱导构象变化,从而对头部和杆状结构域之间的结合产生不利影响。总之,我们的结果表明,自由的 N 端对于纤维组装至关重要,因为 N 端标记的波形蛋白不仅不能形成纤维,而且当整合到预先存在的网络中时也会变得不稳定。